Structure via PubChem · Public domain (PubChem)
diphenyl phosphite
Sign in to saveAlso known as Diphenylphosphite, Phosphonic acid, diphenyl ester
Diphenyl phosphite is a diorganophosphite with the formula (C6H5O)2P(O)H. The molecule is tetrahedral. It is a colorless viscous liquid. The compounds can be prepared by treating phosphorus trichloride with phenol. Many analogues can be prepared similarly. One illustrative reaction, diphenylphosphite, aldehydes, and amines react to afford aminophosphonates (Kabachnik–Fields reaction).
Chemical data
- Formula
- C12H11O3P
- Molecular weight
- 234.19 g/mol
- IUPAC name
- phenoxyphosphonoyloxybenzene
- SMILES
- C1=CC=C(C=C1)OP(=O)OC2=CC=CC=C2
- InChIKey
- OGBPILLJZSJJRC-UHFFFAOYSA-N
- XLogP
- 3.1
- Polar surface area
- 35.5 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 234.045
Show 2 more facts
- canonical SMILES
- C1=CC=C(C=C1)OP(=O)OC2=CC=CC=C2
- chemical formula
- C₁₂H₁₁O₃P
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
Diphenyl phosphite is a diorganophosphite with the formula (C6H5O)2P(O)H. The molecule is tetrahedral. It is a colorless viscous liquid. The compounds can be prepared by treating phosphorus trichloride with phenol. Many analogues can be prepared similarly. One illustrative reaction, diphenylphosphite, aldehydes, and amines react to afford aminophosphonates (Kabachnik–Fields reaction).
==See also== Dimethylphosphite Diethylphosphite Diisopropylphosphite
Excerpted from Wikipedia’s “diphenyl phosphite” article, available under the CC BY-SA 4.0 licence.